Study title:
Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene
Long title:
Phase 3 Randomized, Controlled Study of AAV5-hRKp.RPGR for the Treatment of X-linked Retinitis Pigmentosa Associated with Variants in the RPGR gene
Date receipt dossier:
28 Jan 2022
EU record number:
B/BE/21/BVW8
EudraCT number:
2020-002873-88
Company / Sponsor:
Meira GTx UK II Limited
Phase:
III
Treated organism:
Humans
Indication category:
Genetic disorders
Disease:
X-linked Retinitis Pigmentosa associated with Variants in the RPGR gene
Therapeutic approach:
Gene therapy
Genetic modification:
Non-replicating recombinant vector derived from adeno-associated virus AAV 5 carrying the human RPGR gene
Method of transfer of nucleic acid of interest:
Non-replicating recombinant vector derived from adeno-associated virus AAV 5
Administered biological material:
Genetically modified virus
Route of administration:
Subretinal
Locations in Belgium:
UZ Gent
Nr of subjects:
Up to 60 patients overall and 10 patients in Belgium
Foreseen duration:
Start April 2022 with long-term safety follow-up of patients
Type of procedure:
Contained use and Deliberate release
Current status:
Authorized
Information for the public
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Public information according to the provisions of Directive 2001/18/EC
Information related to the decision procedure
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19 April 2022 - The Biosafety Advisory Council issues a positive advice (with conditions) for this deliberate release
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18 May 2022: The Federal Ministers give a final decision (positive with conditions) for this trial